BATF-mediated regulation of exhausted CD8+ T-cell responses and potential implications for chimeric antigen receptor-T therapy

被引:3
作者
Sun, Chao [1 ]
Li, Dan [2 ]
Wang, Zhengxin [1 ]
机构
[1] Fudan Univ, Huashan Hosp, Liver Transplant Ctr, Dept Gen Surg, 12 Urumqi Rd M, Shanghai 200040, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Inst Immunol, Sch Med, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
amplifying CAR-T efficacy; BATF; CD8+T-cell differentiation; chimeric antigen receptor; efficacy; malignant tumors; potency; T-cell exhaustion; T-cell therapy; transcription factor; TRANSCRIPTION FACTOR; DIFFERENTIATION; IMMUNOTHERAPY; PERSISTENCE; CHECKPOINT; PROGENITOR; COOPERATE; SIGNATURE; INFECTION; EXPANSION;
D O I
10.2217/imt-2023-0170
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chimeric antigen receptor (CAR) T-cell therapy for malignant tumors has reached a crucial stage, with recent studies underscoring the role of T-cell exhaustion in determining the efficacy of CAR-T therapy. This trailblazing discovery has opened new avenues to augment the potency of CAR-T therapy. Basic leucine zipper ATF-like transcription factor (BATF) is indispensable in alleviating T-cell exhaustion and is pivotal in the early stages of CD8(+) T-cell differentiation. In cooperation with other transcription factors, it plays a key role in the differentiation and maturation processes of exhausted T cells. A deeper comprehension of BATF's mechanisms in T-cell biology may yield novel insights into amplifying the efficacy of CAR-T therapy.
引用
收藏
页码:331 / 340
页数:10
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